ibuprofen
Generic: ibuprofen
Labeler: aphena pharma solutions - tennessee, llcDrug Facts
Product Profile
Brand Name
ibuprofen
Generic Name
ibuprofen
Labeler
aphena pharma solutions - tennessee, llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ibuprofen 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71610-902
Product ID
71610-902_3467c445-294a-2001-e063-6294a90aef55
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202413
Listing Expiration
2026-12-31
Marketing Start
2024-05-23
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71610902
Hyphenated Format
71610-902
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ibuprofen (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA202413 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 600 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE (71610-902-53)
- 90 TABLET, FILM COATED in 1 BOTTLE (71610-902-60)
- 120 TABLET, FILM COATED in 1 BOTTLE (71610-902-70)
- 180 TABLET, FILM COATED in 1 BOTTLE (71610-902-80)
- 270 TABLET, FILM COATED in 1 BOTTLE (71610-902-92)
Packages (5)
71610-902-53
60 TABLET, FILM COATED in 1 BOTTLE (71610-902-53)
71610-902-60
90 TABLET, FILM COATED in 1 BOTTLE (71610-902-60)
71610-902-70
120 TABLET, FILM COATED in 1 BOTTLE (71610-902-70)
71610-902-80
180 TABLET, FILM COATED in 1 BOTTLE (71610-902-80)
71610-902-92
270 TABLET, FILM COATED in 1 BOTTLE (71610-902-92)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3467c445-294a-2001-e063-6294a90aef55", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["3467b45b-c432-2923-e063-6394a90a1044"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71610-902-53)", "package_ndc": "71610-902-53", "marketing_start_date": "20250501"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-902-60)", "package_ndc": "71610-902-60", "marketing_start_date": "20250501"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71610-902-70)", "package_ndc": "71610-902-70", "marketing_start_date": "20250501"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71610-902-80)", "package_ndc": "71610-902-80", "marketing_start_date": "20250501"}, {"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (71610-902-92)", "package_ndc": "71610-902-92", "marketing_start_date": "20250501"}], "brand_name": "Ibuprofen", "product_id": "71610-902_3467c445-294a-2001-e063-6294a90aef55", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71610-902", "generic_name": "Ibuprofen", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA202413", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20261231"}